Canonical Allele Identifier: CA1345067216

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142813A= , CM000665.2:g.10142813A=	GRCh38
NC_000003.11:g.10184497A= , CM000665.1:g.10184497A=	GRCh37
NC_000003.10:g.10159497A=	NCBI36
NG_008212.3:g.6179A= , LRG_322:g.6179A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.391A=	ENSP00000512434.1:p.Asn131=
ENST00000696143.1:c.391A=	ENSP00000512435.1:p.Asn131=
ENST00000696153.1:c.340+626A=	ENSP00000512444.1:n.340+626A=
ENST00000256474.3:c.340+626A= MANE Select	ENSP00000256474.3:n.340+626A=
ENST00000256474.2:c.340+626A=	ENSP00000256474.2:n.340+626A=
ENST00000345392.2:c.340+626A=	ENSP00000344757.2:n.340+626A=
ENST00000477538.1:n.268A=
NM_000551.3:c.340+626A= , LRG_322t1:c.340+626A=	NP_000542.1:n.340+626A=
NM_198156.2:c.340+626A=	NP_937799.1:n.340+626A=
XM_011534078.1:c.391A=	XP_011532380.1:p.Asn131=
NM_001354723.1:c.391A=	NP_001341652.1:p.Asn131=
NM_000551.4:c.340+626A= MANE Select	NP_000542.1:n.340+626A=
NM_001354723.2:c.391A=	NP_001341652.1:p.Asn131=
NM_198156.3:c.340+626A=	NP_937799.1:n.340+626A=